Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Nilestriol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Nilestriol
Clinical data
Trade namesWei Ni An
Other namesNylestriol; LY-49825; Ethinylestriol cyclopentyl ether; EE3CPE; 17α-Ethynylestriol 3-cyclopentyl ether
Routes of
administration
By mouth
Drug classEstrogen;Estrogen ether
Identifiers
  • (8R,9S,13S,14S,16R,17R)-3-cyclopentyloxy-17-ethynyl-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene-16,17-diol
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC25H32O3
Molar mass380.528 g·mol−1
3D model (JSmol)
  • C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H]([C@]2(C#C)O)O)CCC4=C3C=CC(=C4)OC5CCCC5
  • InChI=1S/C25H32O3/c1-3-25(27)23(26)15-22-21-10-8-16-14-18(28-17-6-4-5-7-17)9-11-19(16)20(21)12-13-24(22,25)2/h1,9,11,14,17,20-23,26-27H,4-8,10,12-13,15H2,2H3/t20-,21-,22+,23-,24+,25+/m1/s1
  • Key:CHZJRGNDJLJLAW-RIQJQHKOSA-N

Nilestriol (INNTooltip International Nonproprietary Name) (brand nameWei Ni An; developmental code nameLY-49825), also known asnylestriol (USANTooltip United States Adopted Name,BANTooltip British Approved Name), is asyntheticestrogen which was patented in 1971[1] and is marketed inChina.[2][3] It is the3-cyclopentylether ofethinylestriol, and is also known asethinylestriol cyclopentyl ether (EE3CPE).[4] Nilestriol is aprodrug of ethinylestriol, and is a morepotent estrogen in comparison.[4] It is described as a slowly-metabolized, long-acting estrogen and derivative ofestriol.[5][6] Nilestriol was assessed in combination withlevonorgestrel for the potential treatment ofpostmenopausalosteoporosis, but this formulation ultimately was not marketed.[7]

See also

[edit]

References

[edit]
  1. ^Official Gazette of the United States Patent and Trademark Office: Patents. U.S. Department of Commerce, Patent and Trademark Office. 1975. p. 1677.
  2. ^Elks J (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 891–.ISBN 978-1-4757-2085-3.
  3. ^"Nilestriol".Drugs.com.
  4. ^abMcGuire W (14 December 2013).Experimental Biology. Springer Science & Business Media. pp. 161–.ISBN 978-1-4757-4673-0.
  5. ^Schoenberg DR (1977).Biochemical Properties of the Cytoplasmic Estrogen Receptors from Immature Rat and Mature Rabbit Uteri (Ph.D. thesis). University of Wisconsin. p. A-17.
  6. ^"Section 10: Obstetrics and gynecology".Excerpta Medica. 1978.
  7. ^Aronson JK (21 February 2009).Meyler's Side Effects of Endocrine and Metabolic Drugs. Elsevier. pp. 173–.ISBN 978-0-08-093292-7.


Estrogens
ERTooltip Estrogen receptor agonists
Progonadotropins
Antiestrogens
ERTooltip Estrogen receptor antagonists
(incl.SERMsTooltip selective estrogen receptor modulators/SERDsTooltip selective estrogen receptor downregulators)
Aromatase inhibitors
Antigonadotropins
Others
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown


Stub icon

Thisdrug article relating to thegenito-urinary system is astub. You can help Wikipedia byexpanding it.

This article about anestrane is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Nilestriol&oldid=1308582150"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp